LUCCHINI, VALERIA

LUCCHINI, VALERIA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 37 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A mouse model of facioscapulohumeral muscular dystrophy 2005 C. LampertiV. LucchiniC. ZeccaN. Bresolin + Book Part (author) -
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction 2009 S. CortiD. RonchiA. BordoniF. FortunatoD. SantoroR. Del BoV. LucchiniV. CrugnolaD. PapadimitriouS. SalaniN. BresolinG.P. Comi + Article (author) -
Bank of DNA, cell lines and nerve-muscle-cardiac tissues 2005 C. LampertiC. ZeccaM.E. FrugugliettiV. LucchiniG.P. ComiA. BordoniF. FortunatoY. Torrente + Book Part (author) -
Caratterizzazione clinica e molecolare della mutazione MERRF A8344G in una famiglia senza coinvolgimento del SNC 2010 V. LucchiniD. RonchiM. G. D'AngeloA. BordoniL. PeverelliN. BresolinG.P. Comi + Conference Object -
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 2011 M. RanieriD. RonchiA. BordoniV. LucchiniF. FortunatoE. FassoneD. TondutiM. RipoloneS. CortiP. VeggiottiG.P. Comi + Article (author) -
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing 2011 F.M.B. MagriR. Del BoM.G.N. D'AngeloA. GovoniS. GandossiniA. BordoniS. TedeschiF.R. FortunatoV. LucchiniM. CeredaS.P CortiN. BresolinG.P. Comi + Article (author) -
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene 2008 D. RonchiA. BordoniR. VirgilioE. FassoneA. DiFonzoM. ServidaV. LucchiniM. MatteoliN. BresolinG.P. Comi + Article (author) -
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 2011 D. RonchiA. CosiA. BordoniV. LucchiniF. FortunatoE. FassoneD. TondutiM. RanieriM. RipoloneS. CortiP. VeggiottiG.P. Comi + Conference Object -
Congenital myopathy with ptosis, ophthalmoplegia and muscle dystrophic changes: a possible sporadic case of myosin heavy chain type IIa myopathy. 2009 V. LucchiniV. CrugnolaM. ServidaA. BordoniD. RonchiN. BresolinG.P. ComiY. Torrente + Conference Object -
COQ 10 deficiency in statin related Myopathy. 2005 C. LampertiV. LucchiniCRUGNOLA, VERONICAN. Bresolin + Article (author) -
Familial amyotrophic lateral sclerosis with a novel Q23R mutation in the copper/zinc superoxide dismutase gene associated with muscle mitochondrial dysfunction 2007 S. CortiA. BordoniD. RonchiD. SantoroD. PapadimitriouC. LampertiV. LucchiniF. MagriM. GuglieriV. CrugnolaN. BresolinG.P. Comi + Article (author) -
Follow-up of a large population of asymptomatic / oligosymptomatic hyperckemic subjects. 2006 M.E. FrugugliettiV.CrugnolaV.LucchiniC.ZeccaC.LampertiG.P.ComiN.Bresolin + Article (author) -
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients 2012 F. MagriR. Del BoA. GovoniA. BordoniV. LucchiniS. CortiN. BresolinG.P. Comi + Article (author) -
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up 2011 F. MagriA. GovoniM.G. D'AngeloR. Del BoA. BordoniTEDESCHI, SABRINAF. FortunatoV. LucchiniS. BonatoC. LampertiY. TorrenteS. CortiN. BresolinG.P. Comi + Article (author) -
IL DIFETTO OSSIDATIVO E LE ALTERAZIONI DEL DNA MITOCONDRIALE IN TOPI TRANSGENICI MODELLO ANIMALE DELLA ATASSIA SPINOCEREBELLARE DI TIPO 1 2012 V. Lucchini Doctoral Thesis -
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 2015 M. RipoloneD. RonchiV. LucchiniI. ColomboL. VillaA. BordoniF. FortunatoS. CortiG.P. Comi + Article (author) -
Incidental Mitochondrial Myopathy 2010 V. CrugnolaV. LucchiniD. RonchiM.G. D'AngeloA. BordoniL. PeverelliN. BresolinG.P. Comi + Conference Object -
Miopatia mitocondriale con fenotipo clinico “limb-girdle”: studio morfologico e biomolecolare 2010 V. LucchiniD. RonchiM. G. D'AngeloA. BordoniL. PeverelliN. BresolinG. P. Comi + Conference Object -
Miopatia progressiva con ptosi, oftalmoplagia e aspetti distrofici alla biopsia muscolare 2009 V. LucchiniV. CrugnolaA. , BordoniD. RonchiN. BresolinG. P. ComiY. Torrente + Conference Object -
Mitochondrial changes in platelets are not related to those in skeletal muscle during human septic shock 2014 A. ProttiF. FortunatoM. PluderiV. LucchiniG.P. ComiL. Gattinoni + Article (author) -